Genome-wide identification and characterization of gene family for RWP-RK transcription factors in wheat (Triticum aestivum L.)

• Published in: PloS one 2018-12, Vol.13 (12), p.e0208409-e0208409
• Main Authors: Kumar, Anuj, Batra, Ritu, Gahlaut, Vijay, Gautam, Tinku, Kumar, Sanjay, Sharma, Mansi, Tyagi, Sandhya, Singh, Krishna Pal, Balyan, Harindra Singh, Pandey, Renu, Gupta, Pushpendra Kumar
• Format: Article
• Language: English
• Subjects: Alternative splicing; Binding sites; Biology and Life Sciences; Biotechnology; Chromosomes; Chromosomes, Plant - genetics; Cloning, Molecular; Deoxyribonucleic acid; DNA; Efficiency; Embryogenesis; Embryonic growth stage; Evolution, Molecular; Exons; Gametogenesis; Gene expression; Gene Expression Profiling; Gene Expression Regulation, Plant; Genes; Genes, Plant; Genomes; Genotypes; Homology; Identification; Kinases; Multigene Family; Nitrates; Nitrogen; Nitrogen - metabolism; Phylogeny; Physical Sciences; Physiology; Plant Proteins - genetics; Plant tissues; Proteins; Research and Analysis Methods; Rice; Roots; Seedlings; Shoots; Signal transduction; Simple sequence repeats; Simulation analysis; Tobacco; Transcription factors; Transcription Factors - genetics; Transduction; Triticum - genetics; Triticum - metabolism; Wheat; Whole Genome Sequencing
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0208409

RWP-RKs represent a small family of transcription factors (TFs) that are unique to plants and function particularly under conditions of nitrogen starvation. These RWP-RKs have been classified in two sub-families, NLPs (NIN-like proteins) and RKDs (RWP-RK domain proteins). NLPs regulate tissue-specific expression of genes involved in nitrogen use efficiency (NUE) and RKDs regulate expression of genes involved in gametogenesis/embryogenesis. During the present study, using in silico approach, 37 wheat RWP-RK genes were identified, which included 18 TaNLPs (2865 to 7340 bp with 4/5 exons), distributed on 15 chromosomes from 5 homoeologous groups (with two genes each on 4B,4D and 5A) and 19 TaRKDs (1064 to 5768 bp with 1 to 6 exons) distributed on 12 chromosomes from 4 homoeologous groups (except groups 1, 4 and 5); 2-3 splice variants were also available in 9 of the 37 genes. Sixteen (16) of these genes also carried 24 SSRs (simple sequence repeats), while 11 genes had targets for 13 different miRNAs. At the protein level, MD simulation analysis suggested their interaction with nitrate-ions. Significant differences were observed in the expression of only two (TaNLP1 and TaNLP2) of the nine representative genes that were used for in silico expression analysis under varying levels of N at post-anthesis stage (data for other genes was not available for in silico expression analysis). Differences in expression were also observed during qRT-PCR, when expression of four representative genes (TaNLP2, TaNLP7, TaRKD6 and TaRKD9) was examined in roots and shoots of seedlings (under different conditions of N supply) in two contrasting genotypes which differed in NUE (C306 with low NUE and HUW468 with high NUE). These four genes for qRT-PCR were selected on the basis of previous literature, level of homology and the level of expression (in silico study). In particular, the TaNLP7 gene showed significant up-regulation in the roots and shoots of HUW468 (with higher NUE) during N-starvation; this gene has already been characterized in Arabidopsis and tobacco, and is known to be involved in nitrate-signal transduction pathway.